Sistonen P - Search Results

1

Choroideremia: linkage analysis with physically mapped close DNA-markers.

Sankila EM, Sistonen P, Cremers F, de la Chapelle A. Sankila EM, et al. Among authors: sistonen p. Hum Genet. 1991 Jul;87(3):348-52. doi: 10.1007/BF00200918. Hum Genet. 1991. PMID: 1677924

2

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland.

Hästbacka J, de la Chapelle A, Kaitila I, Sistonen P, Weaver A, Lander E. Hästbacka J, et al. Among authors: sistonen p. Nat Genet. 1992 Nov;2(3):204-11. doi: 10.1038/ng1192-204. Nat Genet. 1992. PMID: 1345170

3

Hemophilia A: genetic prediction and linkage studies in all available families in Finland.

Lehesjoki AE, Sistonen P, Rasi V, de la Chapelle A. Lehesjoki AE, et al. Among authors: sistonen p. Clin Genet. 1991 Mar;39(3):199-209. doi: 10.1111/j.1399-0004.1991.tb03012.x. Clin Genet. 1991. PMID: 2036741

4

Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophy.

Lindlöf M, Sistonen P, de la Chapelle A. Lindlöf M, et al. Among authors: sistonen p. Ann Hum Genet. 1987 Oct;51(4):317-28. doi: 10.1111/j.1469-1809.1987.tb01066.x. Ann Hum Genet. 1987. PMID: 3482147

5

The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulator.

Kere J, Sistonen P, Holmberg C, de la Chapelle A. Kere J, et al. Among authors: sistonen p. Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10686-9. doi: 10.1073/pnas.90.22.10686. Proc Natl Acad Sci U S A. 1993. PMID: 7504277 Free PMC article.

6

Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.

Höglund P, Sistonen P, Norio R, Holmberg C, Dimberg A, Gustavson KH, de la Chapelle A, Kere J. Höglund P, et al. Among authors: sistonen p. Am J Hum Genet. 1995 Jul;57(1):95-102. Am J Hum Genet. 1995. PMID: 7611301 Free PMC article.

7

Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

Sankila EM, Pakarinen L, Kääriäinen H, Aittomäki K, Karjalainen S, Sistonen P, de la Chapelle A. Sankila EM, et al. Among authors: sistonen p. Hum Mol Genet. 1995 Jan;4(1):93-8. doi: 10.1093/hmg/4.1.93. Hum Mol Genet. 1995. PMID: 7711740

8

Genetic homogeneity of cartilage-hair hypoplasia.

Sulisalo T, van der Burgt I, Rimoin DL, Bonaventure J, Sillence D, Campbell JB, Chitayat D, Scott CI, de la Chapelle A, Sistonen P, et al. Sulisalo T, et al. Among authors: sistonen p. Hum Genet. 1995 Feb;95(2):157-60. doi: 10.1007/BF00209394. Hum Genet. 1995. PMID: 7860061

9

Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.

Tahvanainen E, Norio R, Karila E, Ranta S, Weissenbach J, Sistonen P, de la Chapelle A. Tahvanainen E, et al. Among authors: sistonen p. Nat Genet. 1994 Jun;7(2):201-4. doi: 10.1038/ng0694-201. Nat Genet. 1994. PMID: 7920642

10

High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia gene.

Sulisalo T, Klockars J, Mäkitie O, Francomano CA, de la Chapelle A, Kaitila I, Sistonen P. Sulisalo T, et al. Among authors: sistonen p. Am J Hum Genet. 1994 Nov;55(5):937-45. Am J Hum Genet. 1994. PMID: 7977356 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

125 results

Search Page

Filters